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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383909Generated: October 25, 2026

Chloroform → Ethyl 2-chloro-5-phenylthiazole-4-carboxylate

https://huagongshe.com/reaction/383909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantIsoamyl nitrateHCID 10985—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-amino-5-phenyl-1,3-thiazole-4-carboxylateHCID 12603728—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-chloro-5-phenylthiazole-4-carboxylateHCID 59291332—

Reaction Steps

To a solution of ethyl 2-amino-5-phenylthiazole-4-carboxylate in MeCN was added CuCl2 at 0° C., and the isoamyl nitrate was slowly added dropwise thereto, followed by stirring for 1 hour. To the reaction mixture was added CHCl3, followed by stirring at 0° C. for 2 hours and then at room temperature for 2 hours. The reaction mixture was neutralized by addition of a 1 M aqueous NaOH solution, and filtered through Celite. The filtrate was extracted with EtOAc, and the organic layer was washed with water and brine in this order and then dried over MgSO4. After concentration under reduced pressure, the residue obtained was purified by medium-pressure preparative liquid chromatography (silica gel YAMAZEN YFLC WPrep2XY, hexane:EtOAc) to obtain ethyl 2-chloro-5-phenylthiazole-4-carboxylate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367696B2
Source datasetuspto-grants-2013_02
ORD IDord-0c053e4a2d1c430b8f52df4f7ffa7ef9
Source noteuspto-grants-2013_02